S. Khaliq

发表

Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant

K. Kidd, J. Kidd, E. Rogaev, 2009, Annals of human genetics.

Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia.

K. Kidd, J. Kidd, S. Q. Mehdi, 2007, American journal of human genetics.

The Kalash Genetic Isolate: Ancient Divergence, Drift, and Selection

C. Tyler-Smith, L. Pagani, S. Q. Mehdi, 2015, American journal of human genetics.

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2

Colin A. Johnson, S. Q. Mehdi, Q. Ayub, 2007, American journal of medical genetics. Part A.

Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu)

S. Bhattacharya, S. Bhattacharya, S. Khaliq, 1999, Human mutation.

Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children.

S. Q. Mehdi, S. Khaliq, S. Naqvi, 2012, Gene.

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa

S. Khaliq, A. Mohyuddin, A. Hameed, 2005, Journal of Medical Genetics.

Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome

S. Khaliq, S. Hashmi, A. Abid, 2018, Front. Genet..

Analysis of FANCC gene mutations (IVS4+4A>T, del322G, and R548X)in patients with Fanconi anemia in Pakistan.

S. Khaliq, S. Jahan, S. Khaliq, 2017, Turkish journal of medical sciences.

A Study of Angiotensin Converting Enzyme ( ACE ) Gene Polymorphism in Essential Hypertension among a Business Community in Punjab

Q. Ayub, S. Khaliq, M. Nasir, 2015 .

DC-SIGN Interacts with Mycobacterium leprae but Sequence Variation in This Lectin Is Not Associated with Leprosy in the Pakistani Population

L. Quintana-Murci, L. Barreiro, Hélène Quach, 2006, Human Immunology.

The role of crumbs genes in the vertebrate cornea.

T. Mcmahon, R. Yee, S. Khaliq, 2010, Investigative ophthalmology & visual science.

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis

T. Knöpfel, F. Hildebrandt, J. Sayer, 2019, Human Genetics.

Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study

Ayesha Afzal, S. Khaliq, A. Amar, 2020, BMC Medical Genetics.

Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease

M. Naveed, S. Khaliq, Nadir Ali, 2022, Genes.

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

A. Bird, G. Holder, S. Bhattacharya, 2004, Archives of ophthalmology.

Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.

S. Bhattacharya, S. Khaliq, B. Leroy, 2000, Investigative ophthalmology & visual science.

COMPARISON OF ANTHROPOMETRIC PARAMETERS BETWEEN OBESE MALE PARTICIPANTS WITH AND WITHOUT OBSTRUCTIVE SLEEP APNEA

S. Khaliq, K. Iqbal, Muniza Saeed, 2021, Journal of University Medical & Dental College.

Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene

K. Kidd, J. Kidd, A. Pakstis, 2008, The Pharmacogenomics Journal.

Two homozygous missense mutations in ITGB3 gene as a cause of Glanzmann Thrombasthenia in four consanguineous Pakistani pedigrees

S. Khaliq, Saima Farhan, A. Amar, 2020, International journal of laboratory hematology.

Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.

S. Q. Mehdi, S. Khaliq, A. Abid, 2011, Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.

Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and essential hypertension in young Pakistani patients.

Q. Ayub, S. Khaliq, M. Nasir, 2004, Journal of biochemistry and molecular biology.

DHPLC Applications: Finding DNA Variation on the Y Chromosome

Q. Ayub, S. Khaliq, A. Mohyuddin, 2003 .

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes

S. Q. Mehdi, S. Khaliq, A. Abid, 2006, Journal of Human Genetics.

The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients.

S. Q. Mehdi, S. Khaliq, T. Aziz, 2012, Gene.

The Origins of Pakistani Populations

M. Hammer, P. Underhill, L. Cavalli-Sforza, 1999 .

Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.

S. Khaliq, A. Abid, S. Shahid, 2011, JPMA. The Journal of the Pakistan Medical Association.

Frequency of CCR5 Gene 32-bp deletion in Pakistani ethnic groups.

S. Q. Mehdi, Q. Ayub, S. Khaliq, 2002, Genetic testing.

The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection

S. Q. Mehdi, S. Khaliq, T. Aziz, 2017, Inflammation Research.

Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection

S. Khaliq, T. Aziz, S. Mahmood, 2017, Immunological investigations.

Response to Hellenthal et al.

C. Tyler-Smith, L. Pagani, S. Q. Mehdi, 2016, American journal of human genetics.

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin

S. Bhattacharya, P. Francis, S. Khaliq, 1999, Human Genetics.

Role of Ecologic ACE I/D Polymorphism Data Towards Prediction of COVID-19 Epidemiology

S. Khaliq, A. Amar, A. Abid, 2021 .

Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis.

S. Q. Mehdi, S. Khaliq, A. Hashmi, 2016, Urologic oncology.

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

S. Bhattacharya, S. Khaliq, A. Hameed, 1999, The British journal of ophthalmology.

HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association

S. Khaliq, T. Aziz, A. Abid, 2022, Human mutation.

Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants

M. Zafar, S. Khaliq, S. Hashmi, 2022, Clinical genetics.

A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

S. Khaliq, S. Bhattacharya, A. Hameed, 1998, American journal of human genetics.

A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.

S. Bhattacharya, S. Khaliq, S. Bhattacharya, 1999, Investigative ophthalmology & visual science.

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.

M. Brodsky, S. Q. Mehdi, M. Dattani, 2012, Human molecular genetics.

“Like sugar in milk”: reconstructing the genetic history of the Parsi population

C. Tyler-Smith, S. Q. Mehdi, Q. Ayub, 2017, bioRxiv.

Reconstruction of human evolutionary tree using polymorphic autosomal microsatellites.

L. Cavalli-Sforza, A. Piazza, Q. Ayub, 2003, American journal of physical anthropology.

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.

S. Q. Mehdi, S. Khaliq, J. Kazi, 2012, Gene.

with recessive cone-rod dystrophy gene mutations associated RPGRIP1 Evidence of

S. Khaliq, A. Hameed, A. Abid, 2007 .

Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy

S. Khaliq, A. Hameed, A. Abid, 2003, Journal of medical genetics.

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

C. Cepko, S. Bhattacharya, S. Daiger, 2000, Nature Genetics.

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations

Colin A. Johnson, S. Q. Mehdi, T. Forshew, 2005, Human Genetics.

FANCA Gene in Pakistani Fanconi Anemia Patients: Screening of Mutations in Exon 28 and Exon 29

S. Jahan, S. Khaliq, Nadir Ali, 2019 .

Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan

Chris Tyler-Smith, Peter A Underhill, Qasim Ayub, 2007, European Journal of Human Genetics.

Investigation of the Greek ancestry of populations from northern Pakistan

L. Cavalli-Sforza, Q. Ayub, S. Khaliq, 2004, Human Genetics.

“Like sugar in milk”: reconstructing the genetic history of the Parsi population

C. Tyler-Smith, S. Q. Mehdi, Q. Ayub, 2017, Genome Biology.

P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients.

Q. Ayub, S. Khaliq, A. Mohyuddin, 2000, Genetic testing.

HLA class I and II polymorphisms in the Gujjar population from Pakistan

S. Q. Mehdi, S. Khaliq, A. Mohyuddin, 2013, Immunological investigations.

HLA polymorphism in six ethnic groups from Pakistan.

S. Q. Mehdi, Q. Ayub, S. Khaliq, 2002, Tissue antigens.

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

S. Q. Mehdi, S. Khaliq, M. Mubarak, 2014, Mutation research.

Independent and Combined Associations of 677C/T and 1298A/C Polymorphisms in the MTHFR gene with Breast Cancers in a South-Asian Population

S. Khaliq, A. Siddiqa, M. Memon, 2021, medRxiv.

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

S. Khaliq, B. Leroy, S. Bhattacharya, 2001, Investigative ophthalmology & visual science.

Absence of Glutathione S-Transferase Theta 1 Gene Is Significantly Associated With Breast Cancer Susceptibility in Pakistani Population and Poor Overall Survival in Breast Cancer Patients: A Case-Control and Case Series Analysis

S. Khaliq, A. Siddiqa, M. Memon, 2021, Frontiers in Oncology.

Locus heterogeneity and Knobloch syndrome

S. Khaliq, L. Tee, E. Maher, 2010, American journal of medical genetics. Part A.

Relationship between IQ and academic performance of medical students.

S. Khaliq, K. Iqbal, S. Chaudhry, 2021 .

Polymorphisms in the methylene tetrahydrofolate reductase gene and their unique combinations are associated with an increased susceptibility to the renal cancers.

S. Q. Mehdi, S. Khaliq, A. Hashmi, 2012, Genetic testing and molecular biomarkers.

In Silico Analysis of NPHS1 Gene Mutations Identified in Patients with Steroid Resistant Nephrotic Syndrome

S. Khaliq, 2017 .

Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis

Ayesha Afzal, S. Khaliq, A. Amar, 2019, Urolithiasis.

FASTING SERUM RESISTIN AND BLOOD GLUCOSE LEVELS IN NEWLY DIAGNOSED MALE PATIENTS OF PULMONARY TUBERCULOSIS WITH AND WITHOUT DIABETES MELLITUS TYPE 2

S. Khaliq, Muniza Saeed, S. Naz, 2020, Pakistan Postgraduate Medical Journal.

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

S. Bhattacharya, S. Khaliq, A. Hameed, 1999, American journal of human genetics.

Analysis of CYP2C9 polymorphisms (*2 and *3) in warfarin therapy patients in Pakistan. Association of CYP2C9 polymorphisms (*2 and*3) with warfarin dose, age, PT and INR

Waqas Latif, S. Khaliq, W. Latif, 2015, Journal of Thrombosis and Thrombolysis.

Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome 17p12-13.3

S. Bhattacharya, S. Khaliq, A. Hameed, 1999 .

Serum vitamin D levels and gene polymorphisms (Fok1 and Apa1) in children with type I diabetes and healthy controls.

S. Khaliq, S. Khaliq, K. Lone, 2016, JPMA. The Journal of the Pakistan Medical Association.

African and Levantine origins of Pakistani YAP+ Y chromosomes.

M. Hammer, S. Q. Mehdi, Q. Ayub, 1999, Human biology.

A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.

S. Khaliq, S. Bhattacharya, A. Hameed, 2001, Investigative ophthalmology & visual science.

Mutation screening of Pakistani families with congenital eye disorders.

S. Q. Mehdi, S. Khaliq, A. Mohyuddin, 2003, Experimental eye research.

RP1 protein truncating mutations predominate at the RP1 adRP locus.

A. Bird, S. Bhattacharya, E. Vithana, 2000, Investigative ophthalmology & visual science.

RP 1 Protein Truncating Mutations Predominate at the RP 1 adRP Locus

A. Bird, S. Bhattacharya, E. Vithana, 2000 .

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis

T. Knöpfel, F. Hildebrandt, J. Sayer, 2019, Human Genetics.

Perspectives on Human Genome Diversity within Pakistan using Y Chromosomal and Autosomal Microsatellite Markers

C. Tyler-Smith, L. Cavalli-Sforza, S. Q. Mehdi, 2002 .

A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.

S. Khaliq, A. Hameed, M. Ismail, 2001, Investigative ophthalmology & visual science.

Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases

S. Khaliq, A. Abid, M. Ismail, 2005, Journal of Medical Genetics.

gene associated with retinal degenerative diseases SEMA4A Identification of novel mutations in the

S. Khaliq, A. Abid, M. Ismail, 2006 .

Association of a single-nucleotide polymorphism in the promoter region of the VEGF gene with the risk of renal cell carcinoma.

S. Q. Mehdi, S. Khaliq, A. Hashmi, 2011, Genetic testing and molecular biomarkers.

Association of specific single nucleotide variants (SNVs) in the promoter and 3'-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers.

S. Khaliq, A. Siddiqa, A. Abid, 2021, Oral oncology.

Strong and Significant Associations of Single Nucleotide Variants (SNVs) in the Promoter and 3'-Untranslated Region (3'-UTR) of Vascular Endothelial Growth Factor (VEGF) Gene with Head and Neck Cancers

S. Khaliq, A. Siddiqa, M. Memon, 2021, medRxiv.

Host Genetic and Epigenetic Factors in Determining Clinical Outcome of Coronavirus Disease-2019

S. Khaliq, A. Amar, Tanveer Khalid, 2020, BioMedica.

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

S. Khaliq, M. Mubarak, A. Hashmi, 2014, Mutation research.

Association analysis of the VEGF gene variants with breast cancer susceptibility and tumor characteristics in an indigenous population: A pilot study

S. Khaliq, A. Siddiqa, M. Memon, 2019, Gene Reports.

Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene

K. Kidd, J. Kidd, A. Pakstis, 2008, The Pharmacogenomics Journal.